Canonical Allele Identifier: CA15402046
Gene: LINC01933 HGNC NCBI
COSMIC:
COSN14902169 (not active)
MyVariant.info:
GRCh38 chr5:g.151964997G>A
GRCh37 chr5:g.151344558G>A
gnomAD v2:
5:151344558 G / A
gnomAD v3:
5:151964997 G / A
gnomAD v4:
chr5-151964997-G-A
Joint Max Group AF 0.72725619 (AFR)
Genomes Max Group AF 0.72725619 (AFR)
dbSNP:
170020
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151964997G>A , CM000667.2:g.151964997G>A GRCh38
NC_000005.9:g.151344558G>A , CM000667.1:g.151344558G>A GRCh37
NC_000005.8:g.151324751G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109876.1:n.57+6043G>A
Search 100 bp 5'
Search 100 bp 3'